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TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik
|
November 9, 2013
Dosage response of rye genes in a wheat background : 2. Secalin genes on 1RS
D C Bittel, J P Gustafson
The Journal of Biological Chemistry
|
August 26, 2000
Functional heterogeneity in the zinc fingers of metalloregulatory protein metal response element-binding transcription factor-1
D C Bittel, I V Smirnova, G K Andrews
American Journal of Medical Genetics. Part A
|
August 14, 2008
Analysis of the Prader-Willi syndrome chromosome region using quantitative microsphere hybridization (QMH) array
H L Newkirk, D C Bittel, M G Butler
Journal of Medical Genetics
|
August 16, 2003
Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD
D C Bittel, N Kibiryeva, Z Talebizadeh, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik
|
October 30, 2013
Lysine accumulation in maize cell cultures transformed with a lysine-insensitive form of maize dihydrodipicolinate synthase
D C Bittel, J M Shaver, D A Somers, et al.
The Journal of Biological Chemistry
|
March 29, 2000
Zinc and cadmium can promote rapid nuclear translocation of metal response element-binding transcription factor-1
I V Smirnova, D C Bittel, R Ravindra, et al.
Journal of Autism and Developmental Disorders
|
September 17, 2005
Brief report: non-random X chromosome inactivation in females with autism
Z Talebizadeh, D C Bittel, O J Veatch, et al.
International Journal of Obesity (2005)
|
October 19, 2005
Circulating adiponectin levels, body composition and obesity-related variables in Prader-Willi syndrome: comparison with obese subjects
L Kennedy, D C Bittel, N Kibiryeva, et al.
Journal of Medical Genetics
|
December 25, 2007
Comparison of X-chromosome inactivation patterns in multiple tissues from human females
D C Bittel, M F Theodoro, N Kibiryeva, et al.
Cytogenetic and Genome Research
|
May 8, 2009
Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH
D C Bittel, S Yu, H Newkirk, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 13) with videos related to
Sort By:
Page
of 2
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik
|
November 9, 2013
Dosage response of rye genes in a wheat background : 2. Secalin genes on 1RS
D C Bittel, J P Gustafson
The Journal of Biological Chemistry
|
August 26, 2000
Functional heterogeneity in the zinc fingers of metalloregulatory protein metal response element-binding transcription factor-1
D C Bittel, I V Smirnova, G K Andrews
American Journal of Medical Genetics. Part A
|
August 14, 2008
Analysis of the Prader-Willi syndrome chromosome region using quantitative microsphere hybridization (QMH) array
H L Newkirk, D C Bittel, M G Butler
Journal of Medical Genetics
|
August 16, 2003
Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD
D C Bittel, N Kibiryeva, Z Talebizadeh, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik
|
October 30, 2013
Lysine accumulation in maize cell cultures transformed with a lysine-insensitive form of maize dihydrodipicolinate synthase
D C Bittel, J M Shaver, D A Somers, et al.
The Journal of Biological Chemistry
|
March 29, 2000
Zinc and cadmium can promote rapid nuclear translocation of metal response element-binding transcription factor-1
I V Smirnova, D C Bittel, R Ravindra, et al.
Journal of Autism and Developmental Disorders
|
September 17, 2005
Brief report: non-random X chromosome inactivation in females with autism
Z Talebizadeh, D C Bittel, O J Veatch, et al.
International Journal of Obesity (2005)
|
October 19, 2005
Circulating adiponectin levels, body composition and obesity-related variables in Prader-Willi syndrome: comparison with obese subjects
L Kennedy, D C Bittel, N Kibiryeva, et al.
Journal of Medical Genetics
|
December 25, 2007
Comparison of X-chromosome inactivation patterns in multiple tissues from human females
D C Bittel, M F Theodoro, N Kibiryeva, et al.
Cytogenetic and Genome Research
|
May 8, 2009
Refining the 22q11.2 deletion breakpoints in DiGeorge syndrome by aCGH
D C Bittel, S Yu, H Newkirk, et al.
Page
of 2